Oliver’s Story with SynGAP
Patient Worthy is honored to share Oliver's story on behalf of SynGAP Research Fund. SRF is a global group of families committed to accelerating the science to cure SYNGAP1 &…
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Oliver’s Story with SynGAP
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Utah Researcher is Screening Thousands of Drugs to Identify Potential SYNGAP1 Treatment
It can be undoubtedly difficult to identify therapies for rare diseases. Between the cost of research, the small population sizes, and the time required, the drug development process can…
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Utah Researcher is Screening Thousands of Drugs to Identify Potential SYNGAP1 Treatment
Their Child Has SYNGAP1 Syndrome, Causing the Family to Face Overwhelming Challenges
Perhaps one of the most difficult challenges of families impacted by certain rare diseases is trying to appear “normal” for the sake of others in the family. That is one…
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Their Child Has SYNGAP1 Syndrome, Causing the Family to Face Overwhelming Challenges
